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  5. NDC Package Code: 64406-560-01 Guselkumab

NDC Package 64406-560-01 Guselkumab

Liquid - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
64406-560-01
Package Description:
10 kg in 1 BOTTLE
Product Code:
64406-560
Non-Proprietary Name:
Guselkumab
Substance Name:
Guselkumab
Usage Information:
This medication is used to treat plaque psoriasis and psoriatic arthritis. Guselkumab belongs to a class of drugs known as monoclonal antibodies. It works by blocking a certain natural substance in your body (interleukin-23) that may cause inflammation and swelling. Guselkumab can help lessen the red, scaly, itchy patches of skin caused by plaque psoriasis and lessen the pain and swelling in the joints caused by psoriatic arthritis.
11-Digit NDC Billing Format:
64406056001
Product Type:
Bulk Ingredient
Labeler Name:
Biogen Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Active Ingredient(s):
GUSELKUMAB 10 kg/10kg
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
07-13-2017
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Unfinished Product:
Yes
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 64406-560-01?

The NDC Packaged Code 64406-560-01 is assigned to an UNFINISHED drug package of 10 kg in 1 bottle of Guselkumab, a bulk ingredient labeled by Biogen Inc.. The product's dosage form is liquid and is administered via form.

Is NDC 64406-560 included in the NDC Directory?

Yes, Guselkumab is an UNFINISHED PRODUCT with code 64406-560 that is active and included in the NDC Directory. The product was first marketed by Biogen Inc. on July 13, 2017 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 64406-560-01?

The 11-digit format is 64406056001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-264406-560-015-4-264406-0560-01